chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1432052183205219GA43GENIChomozygous970760906
1432052253205226GT38GENIChomozygous970760907
1432056643205665CT19GENIChomozygous970760908
1432063373206338CA38GENIChomozygous970760909
1432081793208180CT23GENIChomozygous970760910
1432134853213486TG26GENIChomozygous970760911
1432150703215071AG28GENIChomozygous970760912
1432153673215368TC35GENIChomozygous970760913
1432160573216058GA29GENIChomozygous970760914
1432161473216148TA26GENIChomozygous970760915
1432169313216932GT36GENIChomozygous970760916
1432184303218431AG33GENIChomozygous970760917
1432208893220890GA41GENIChomozygous970760918
1432209233220924TC36GENIChomozygous970760919
1432213363221337CT24GENIChomozygous970760920
1432226683222669CT37GENIChomozygous970760921
1432228023222803GT20GENIChomozygous970760922
1432239873223988CT24GENIChomozygous970760923
1432254713225472CT31GENIChomozygous970760924
1432266743226675AG31GENICpossibly homozygous970760925
1432293013229302TC34GENIChomozygous970760926
1432314983231499TC33GENIChomozygous970760927
1432321093232110AC15GENIChomozygous970760928
1432428213242822AC24GENIChomozygous970760929
1432451503245151CT20GENIChomozygous970760930
1432455153245516GA29GENICpossibly homozygous970760931
1432455893245590AG36GENIChomozygous970760932
1432456843245685GA32GENIChomozygous970760933
1432469093246910AG27GENIChomozygous970760934
1432470153247016TC36GENIChomozygous970760935